About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Prader-Willi Syndrome; PWS
OMIM ID: 176270
Human Phenotype Ontology associations
View all models View ALL (19) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     MAGEL2* Magel2* View 2 models HomoloGene and HGNC
NDN* Ndn* View 7 models HomoloGene and HGNC
SNRPN* Snrpn* View 3 models HomoloGene and HGNC
     HTR2C Htr2c* View 1 model HomoloGene and HGNC
     HERC2* Herc2   HomoloGene and HGNC
MKRN3* Mkrn3   HomoloGene and HGNC
NPAP1*   HomoloGene
SNORD115-1*   HGNC
SNORD116-1*   HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Del(7Herc2-Mkrn3)13FRdni View 1 model
  Snord116 View 2 models
  T(7;18)50H View 1 model
  T(7;18)50H View 1 model
  Tg(Igh-Lmp2a)13FRdni View 1 model
References Disease References using Mouse Models (17)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.07
The Jackson Laboratory